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Gut flora profiling in people with cardiovascular disease

Not Applicable
Conditions
cardiovascular disease
Cardiovascular - Coronary heart disease
Cardiovascular - Other cardiovascular diseases
Registration Number
ACTRN12619001727134
Lead Sponsor
Girish Dwivedi
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
All
Target Recruitment
200
Inclusion Criteria

Men and women between the age of 40– 80 years of age presenting to FSH with acute
coronary syndrome or chronic stable angina will be recruited for the study. Healthy family
members of patients will be invited to take part in the study and will act as environmental
controls and will be age matched where possible.

• The participant to present to FSH with acute coronary syndrome or chronic stable
angina.
• Healthy participants will be relatives of ACS patients and are defined as individuals
with no clinically relevant abnormalities identified by a detailed medical history, full
physical examination including blood pressure, heart rate, clinical lab tests from a
fasting blood sample
• Evidence of a personally signed and dated informed consent document indicating that
the participant has been informed of all pertinent aspects of the trial
• Willing and able to comply with study procedures, i.e. sample collection

Exclusion Criteria

Participants will be excluded from the study:
• If there are circumstances that interfere with the participant’s ability to give informed
consent (e.g. diminished understanding, or proficiency in English language and an
interpreter unavailable)
• Participants taking probiotics, antibiotics or antivirals which may disrupt gut
microbiota environment, current or recent <3 months.
• Major chronic disease e.g. cancer or dementia
• Healthy participants will be excluded if they have a history of major chronic disease
(including cardiovascular disease, psychiatric illness, cancer, diabetes), BMI <18 or
>35 kg/m2, current or recent (<12 months) smoking, current or recent (<6 months)
significant weight loss or gain (>6% body weight), alcohol intake >280g p/week for
men and >210g p/week for women.
• Inability to comply with study procedure

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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